Have questions? Visit https://www.reddit.com/r/SNPedia

rs180177122

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 7 Fanconi anemia, complementation group N
(A;G) 3 increased risk of breast cancer
(G;G) 0 common in clinvar
ReferenceGRCh38 38.1/141
Chromosome16
Position23626266
GenePALB2
is asnp
is mentioned by
dbSNPrs180177122
ebirs180177122
HLIrs180177122
Exacrs180177122
Varsomers180177122
Maprs180177122
PheGenIrs180177122
hapmaprs180177122
1000 genomesrs180177122
hgdprs180177122
ensemblrs180177122
gopubmedrs180177122
geneviewrs180177122
scholarrs180177122
googlers180177122
pharmgkbrs180177122
gwascentralrs180177122
openSNPrs180177122
23andMers180177122
23andMe allrs180177122
SNP Nexus

SNPshotrs180177122
SNPdbers180177122
MSV3drs180177122
GWAS Ctlgrs180177122
Max Magnitude7
ClinVar
Risk Rs180177122(A;A)
Alt Rs180177122(A;A)
Reference Rs180177122(G;G)
Significance Pathogenic
Disease Familial cancer of breast not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast not provided
Reversed 1
HGVS NC_000016.9:g.23637587C>T
CLNSRC PALB2 database
CLNACC RCV000114552.1, RCV000255170.1,


[PMID 21285249OA-icon.png] Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.